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Updated: Apr 18, 2026

Calcium Carbonate Formation in the Presence of Biopolymeric Additives
Published on: May 14, 2019
Calcium carbonate nucleation driven by ion binding in a biomimetic matrix revealed by in situ electron microscopy
Paul J M Smeets1, Kang Rae Cho2, Ralph G E Kempen3
11] Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA [2] Laboratory of Materials and Interface Chemistry and Soft Matter CryoTEM Unit, Eindhoven University of Technology, PO Box 513, 5600 MB Eindhoven, The Netherlands [3] Institute for Complex Molecular Systems, Eindhoven University of Technology, PO Box 513, 5600 MB Eindhoven, The Netherlands [4] Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
Abstract:
The characteristic shapes, structures and properties of biominerals arise from their interplay with a macromolecular matrix. The developing mineral interacts with acidic macromolecules, which are either dissolved in the crystallization medium or associated with insoluble matrix polymers, that affect growth habits and phase selection or completely inhibit precipitation in solution. Yet little is known about the role of matrix-immobilized acidic macromolecules in directing mineralization. Here, by using in situ liquid-phase electron microscopy to visualize the nucleation and growth of CaCO3 in a matrix of polystyrene sulphonate (PSS), we show that the binding of calcium ions to form Ca-PSS globules is a key step in the formation of metastable amorphous calcium carbonate (ACC), an important precursor phase in many biomineralization systems. Our findings demonstrate that ion binding can play a significant role in directing nucleation, independently of any control over the free-energy barrier to nucleation.
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